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Evaluation of glutathione S‐transferase polymorphisms and mutagen sensitivity as risk factors for the development of second primary tumors in patients previously diagnosed with early‐stage head and neck cancer
Author(s) -
Minard Charles G.,
Spitz Margaret R.,
Wu Xifeng,
Hong Waun Ki,
Etzel Carol J.
Publication year - 2006
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.21928
Subject(s) - medicine , genotype , glutathione s transferase , oncology , confidence interval , bleomycin , head and neck cancer , hazard ratio , mutagen , gastroenterology , cancer , glutathione , genetics , biology , carcinogen , chemotherapy , gene , biochemistry , enzyme
BACKGROUND The objective of this study was to evaluate the effects of polymorphisms in 2 genes in the glutathione S‐transferase (GST) family and the mutagen‐sensitivity phenotype on the risk of second primary tumors (SPTs) in patients with previously diagnosed early‐stage head and neck squamous cell carcinoma. Data were available for 303 patients who were enrolled in a placebo‐controlled chemoprevention trial of low‐dose 13‐ cis ‐retinoic acid to reduce the occurrence of SPTs. METHODS A Cox proportional hazards model and survival tree analysis were used to evaluate the association between specified genetic variations and the development of SPTs. The average number of bleomycin‐induced chromatid breaks per cell was used to quantify mutagen sensitivity as an individual patient's degree of sensitivity to genotoxicity. RESULTS The GST‐M1 null genotype was associated with an increased risk for any SPTs (hazard ratio [HR], 1.99; 95% confidence interval [95% CI], 1.11‐3.56) and for tobacco‐related SPTs (HR, 2.16; 95% CI, 1.01‐4.62) after adjusting for covariates. The GST‐T1 null genotype and bleomycin‐induced chromatid breaks were not associated with a statistically significant increased risk for SPTs or tobacco‐related SPTs after similar adjustment. Simultaneous nonnull status for both GST genotypes was associated with a decreased risk for any SPTs (HR, 0.52; 95% CI, 0.28‐0.96) and tobacco‐related SPTs (HR, 0.50; 95% CI, 0.22‐1.11) compared with null status for GST‐M1 accompanied by nonnull status for GST‐T1. CONCLUSIONS An association was observed between the development of SPTs and the GST‐M1 null genotype after successful treatment for early‐stage head and neck squamous cell carcinoma. The GST‐T1 null genotype and bleomycin‐induced chromatid breaks were not associated with an increased risk, and no significant interactions were identified. Cancer 2006. © 2006 American Cancer Society.